Optimisation des performances et de la robustesse d’un électrolyseur à hautes températures

The thermal, electrochemical and mechanical response of a high temperature steam electrolyzer (HTSE) has been analyzed in this work. To this end, a multi-physics and multi-scale modelling approach has been employed: • A local model, at the microstructure scale of the electrodes, has been used to analyze the apparent electrochemical behavior of the electrodes related to the studied electrolysis cell. System operation, in a stack of several cells, has been then analyzed using a thermoelectrochemical model at the macroscopic scale of the HTSE. An element of experimental validation of the model comes with the results. • A thermomechanical model for the calculation of the stress state of the HTSE has been developed. In this model, the intrinsic physical phenomena of the cell, of its operation under current at high temperatures and those ascribable to the mechanical interactions between the cell and its environment have been considered. The unknown data required for the models have been obtained by the characterization and homogenization calculations of the three-dimensional microstructure of the electrodes. Besides, the viscoplastic behavior of the cathode material has been determined by a four-point bending creep test. The study made it possible to define an optimal operating zone, ensuring both high electrochemical performances and acceptable temperature levels. Proposals aiming to reduce the mechanical damage of the system have been also produced.La réponse thermique, électrochimique et mécanique d'un électrolyseur de la vapeur d'eau à haute température (EVHT) a été analysée dans ce travail. Pour ce faire, une approche de modélisation multi-physique et multi-échelle a été employée : • Un modèle local, à l'échelle de la microstructure des électrodes, a été utilisé pour analyser le comportement électrochimique apparent des électrodes de la cellule d'électrolyse étudiée. Le fonctionnement du système au sein d'un empilement de plusieurs cellules a ensuite été analysé grâce à un modèle thermoélectrochimique à l'échelle macroscopique de l'EVHT. Un élément de validation expérimentale du modèle accompagne les résultats. • Un modèle thermomécanique pour le calcul de l'état de contrainte de l'EVHT a été développé. Celui-ci tient compte des phénomènes physiques intrinsèques à la cellule et à son fonctionnement sous courant à hautes températures et à ceux imputables aux interactions mécaniques entre la cellule et son environnement. Les données manquantes nécessaires à l'exécution des modèles ont été obtenues par la caractérisation et par des calculs d'homogénéisation de la microstructure tridimensionnelle des électrodes. Par ailleurs le comportement viscoplastique du matériau de la cathode a été mis évidence par des essais de fluage en flexion quatre points. L'étude a permis de définir un domaine de fonctionnement optimal garantissant des performances électrochimiques élevées avec des niveaux de température acceptables. Des propositions visant à réduire l'endommagement mécanique du système ont également été produites

Quantitative Relationships Between Pore Tortuosity, Pore Topology, and Solid Particle Morphology Using a Novel Discrete Particle Size Algorithm

To sustain the continuous high-rate charge current required for fast charging of electric vehicle batteries, the ionic effective diffusion coefficient of the electrodes must be high enough to avoid the electrode being transport limited. Tortuosity factor and porosity are the two microstructure parameters that control this effective diffusion coefficient. While different methods exist to experimentally measure or calculate the tortuosity factor, no generic relationship between tortuosity and microstructure presently exists that is applicable across a large variety of electrode microstructures and porosities. Indeed, most relationships are microstructure specific. In this work, generic relationships are established using only geometrically defined metrics that can thus be used to design thick electrodes suitable for fast charging. To achieve this objective, an original, discrete particle-size algorithm is introduced and used to identify and segment particles across a set of 19 various electrode microstructures (nickel-manganese-cobalt [NMC] and graphite) obtained from X-ray computed tomography (CT) to quantify parameters such as porosity, particle elongation, sinuosity, and constriction, which influence the effective diffusion coefficient. Compared to the widely used watershed method, the new algorithm shows less over-segmentation. Particle size obtained with different numerical methods is also compared. Lastly, microstructure-tortuosity relationship and particle size and morphology analysis methods are reviewed

Resolving the Discrepancy in Tortuosity Factor Estimation for Li-Ion Battery Electrodes through Micro-Macro Modeling and Experiment

Battery performance is strongly correlated with electrode microstructural properties. Of the relevant properties, the tortuosity factor of the electrolyte transport paths through microstructure pores is important as it limits battery maximum charge/discharge rate, particularly for energy-dense thick electrodes. Tortuosity factor however, is difficult to precisely measure, and thus its estimation has been debated frequently in the literature. Herein, three independent approaches have been applied to quantify the tortuosity factor of lithium-ion battery electrodes. The first approach is a microstructure model based on three-dimensional geometries from X-ray computed tomography (CT) and stochastic reconstructions enhanced with computationally generated carbon/binder domain (CBD), as CT is often unable to resolve the CBD. The second approach uses a macro-homogeneous model to fit electrochemical data at several rates, providing a separate estimation of the tortuosity factor. The third approach experimentally measures tortuosity factor via symmetric cells employing a blocking electrolyte. Comparisons have been made across the three approaches for 14 graphite and nickel-manganese-cobalt oxide electrodes. Analysis suggests that if the tortuosity factor were characterized based on the active material skeleton only, the actual tortuosities would be 1.35–1.81 times higher for calendered electrodes. Correlations are provided for varying porosity, CBD phase interfacial arrangement and solid particle morphology

Optimization of the performances and the robustness of an electrolyser at high temperatures

La réponse thermique, électrochimique et mécanique d'un électrolyseur de la vapeur d'eau à haute température (EVHT) a été analysée dans ce travail. Pour ce faire, une approche de modélisation multi-physique et multi-échelle a été employée : • Un modèle local, à l'échelle de la microstructure des électrodes, a été utilisé pour analyser le comportement électrochimique apparent des électrodes de la cellule d'électrolyse étudiée. Le fonctionnement du système au sein d'un empilement de plusieurs cellules a ensuite été analysé grâce à un modèle thermoélectrochimique à l'échelle macroscopique de l'EVHT. Un élément de validation expérimentale du modèle accompagne les résultats. • Un modèle thermomécanique pour le calcul de l'état de contrainte de l'EVHT a été développé. Celui-ci tient compte des phénomènes physiques intrinsèques à la cellule et à son fonctionnement sous courant à hautes températures et à ceux imputables aux interactions mécaniques entre la cellule et son environnement. Les données manquantes nécessaires à l'exécution des modèles ont été obtenues par la caractérisation et par des calculs d'homogénéisation de la microstructure tridimensionnelle des électrodes. Par ailleurs le comportement viscoplastique du matériau de la cathode a été mis évidence par des essais de fluage en flexion quatre points. L'étude a permis de définir un domaine de fonctionnement optimal garantissant des performances électrochimiques élevées avec des niveaux de température acceptables. Des propositions visant à réduire l'endommagement mécanique du système ont également été produites.The thermal, electrochemical and mechanical response of a high temperature steam electrolyzer (HTSE) has been analyzed in this work. To this end, a multi-physics and multi-scale modelling approach has been employed: • A local model, at the microstructure scale of the electrodes, has been used to analyze the apparent electrochemical behavior of the electrodes related to the studied electrolysis cell. System operation, in a stack of several cells, has been then analyzed using a thermoelectrochemical model at the macroscopic scale of the HTSE. An element of experimental validation of the model comes with the results. • A thermomechanical model for the calculation of the stress state of the HTSE has been developed. In this model, the intrinsic physical phenomena of the cell, of its operation under current at high temperatures and those ascribable to the mechanical interactions between the cell and its environment have been considered. The unknown data required for the models have been obtained by the characterization and homogenization calculations of the three-dimensional microstructure of the electrodes. Besides, the viscoplastic behavior of the cathode material has been determined by a four-point bending creep test. The study made it possible to define an optimal operating zone, ensuring both high electrochemical performances and acceptable temperature levels. Proposals aiming to reduce the mechanical damage of the system have been also produced

Enabling fast charging of lithium-ion batteries through secondary- /dual- pore network: Part I - Analytical diffusion model

Battery performance is strongly correlated with electrode microstructural properties. Enabling fast charging of lithium-ion batteries requires improved through-plane ionic diffusion that can be achieved through, among other strategies, structured electrodes with a secondary- or dual-pore network (SPN). In this work, an analytical model investigates the impact of such an SPN on ionic diffusion with a composite electrode, considering various pore-channel geometries and comparing to standard electrodes with identical gravimetric- and volumetric-specific theoretical capacities. Relevant SPN design parameters and tortuosity coefficients are identified according to three optimization objectives that aim to balance the improved overall through-plane diffusion, thanks to the coarse aligned channels, and degraded in-plane diffusion because of the porous matrix densification required to maintain gravimetric- and volumetric-specific theoretical capacities. The model indicates that a relatively low amount of SPN is required and that electrodes with high through-plane tortuosity and low in-plane tortuosity benefit most from such architecture

Quantitative microstructure characterization of a Ni-YSZ bi-layer coupled with simulated electrode polarization

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Enabling fast charging of lithium-ion batteries through secondary- /dual- pore network: Part I - Analytical diffusion model

Battery performance is strongly correlated with electrode microstructural properties. Enabling fast charging of lithium-ion batteries requires improved through-plane ionic diffusion that can be achieved through, among other strategies, structured electrodes with a secondary- or dual-pore network (SPN). In this work, an analytical model investigates the impact of such an SPN on ionic diffusion with a composite electrode, considering various pore-channel geometries and comparing to standard electrodes with identical gravimetric- and volumetric-specific theoretical capacities. Relevant SPN design parameters and tortuosity coefficients are identified according to three optimization objectives that aim to balance the improved overall through-plane diffusion, thanks to the coarse aligned channels, and degraded in-plane diffusion because of the porous matrix densification required to maintain gravimetric- and volumetric-specific theoretical capacities. The model indicates that a relatively low amount of SPN is required and that electrodes with high through-plane tortuosity and low in-plane tortuosity benefit most from such architecture

Fingerprinting Redox Heterogeneity in Electrodes during Extreme Fast Charging

Conventionally, battery electrodes are rationalized as homogeneous reactors. It proves to be an erroneous interpretation for fast transients, where mass transport limitations amplify underlying heterogeneities. Given the lack of observability of associated fast spatiotemporal dynamics, redox activity in inhomogeneous electrodes is superficially explored. We resort to a physics-based description to examine extreme fast charging of lithium-ion battery electrodes. Representative inhomogeneity information is extracted from electrode tomograms. We discover such electrodes to undergo preferential intercalation, localized lithium plating and nonuniform heat generation as a result of distributed long- and short-range interactions. The spatial correlations of these events with the underlying inhomogeneity are found to be nonidentical. Investigation of multiple inhomogeneity fields reveals an exponential scaling of plating severity and early onset in contrast to the homogeneous limit. Anode and cathode inhomogeneities couple nonlinearly to grow peculiar electrodeposition patterns. These mechanistic insights annotate the complex functioning of spatially nonuniform electrodes